Establishment registration
NINGBO RISENMED TECHNOLOGY CO.,LTD.
FDA establishment registration 3023339256 · Ningbo Zhejiang, CN
Key facts
| Registration number | 3023339256 |
|---|---|
| Establishment name | NINGBO RISENMED TECHNOLOGY CO.,LTD. |
| Owner/operator | Ningbo Risenmed Technology Co.,Ltd. |
| Owner/operator number | 10085370 |
| FEI number | 3023339256 |
| Address | Room 1636, block a, building 95, No. 586 Jiangnan Road, Yinzhou District |
| City | Ningbo Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BTQ, BYF, BYG, CAE, EXG, EYZ, FMI, FON, FPP, FQZ, FZZ, GAX, HMP, HOY, HSP, HTD, ILH, IME, ITG, JCY, KGO, KGX, KME, KSS, KXF, KYR, KYT, LDE, LRJ, LRR and 12 more |
| Device classes | 1, 2, N |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database